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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2231828생성일: 2026년 10월 26일

Formaldehyde → 6-Methoxy-2-(2,6-dimethylmorpholinomethyl)-1,2,3,4-tetrahydronaphthalen-1-one

https://huagongshe.com/reaction/2231828

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물WaterHCID 962—
반응물6-Methoxy-alpha-tetraloneHCID 14112—
반응물2,6-Dimethylmorpholine hydrochlorideHCID 19374754—
촉매Hydrochloric AcidHCID 313—
용매EthanolHCID 702—
생성물6-Methoxy-2-(2,6-dimethylmorpholinomethyl)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 13770569—

반응 단계

6-Methoxy-1,2,3,4-tetrahydronaphthalen-1-one (17.6 g, 0.1 mol), 2,6-dimethylmorpholine hydrochloride (15.1 g, 0.1 mol), and paraformaldehyde (6.0 g, 0.2 mol) were refluxed together in ethanol (50 ml) with concentrated hydrochloric acid (0.25 ml) as a catalyst for 3 hours. The reaction was cooled and poured into water containing concentrated hydrochloric acid (5 ml) and extracted with ether (200 ml). The aqueous solution was cooled in ice and neutralised with sodium hydroxide solution (10%) then extracted with ether (2×200 ml) dried over magnesium sulphate and evaporated under reduced pressure to give a residue which was recrystallised from petrol (60°-80°) to give 6-methoxy-2-(2,6-dimethylmorpholinomethyl)-1,2,3,4-tetrahydronaphthalen-1-one a white crystalline solid (10 g, 33% yield) melting at 110° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04785006
출처 데이터셋uspto-grants-1988_11
ORD IDord-b4e037832f3844949cd1d2460ced76f7
출처 메모uspto-grants-1988_11